Anti-Cytokeratin/Keratin K3/K76 Monoclonal Antibody

Category: Antibodies
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03-61807
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Product Name Anti-Cytokeratin/Keratin K3/K76 Monoclonal Antibody
Description The protein encoded by this gene is a member of the keratin gene family. The type II cytokeratins consist of basic or neutral proteins which are arranged in pairs of heterotypic keratin chains coexpressed during differentiation of simple and stratified epithelial tissues. This type II cytokeratin is specifically expressed in the corneal epithelium with family member KRT12 and mutations in these genes have been associated with Meesmann's Corneal Dystrophy. The type II cytokeratins are clustered in a region of chromosome 12q12-q13. Mouse Monoclonal Antibody to Keratin K3/K76. Polypeptide reacting: Mr 64 000 polypeptide (keratin K3; formerly also designated cytokeratin 3) of human corneal epithelium and keratin K76 (formerly also designated cytokeratin K2p) of palate epithelium.
Synonyms K3, CK3, KRT76, KRT2B, KRT2P, HUMCYT2A
Clonality Monoclonal
Clone AE5
Immunogen Human epidermal keratin
Isotype IgG1
Specificity AE 5 represents an excellent marker for corneal type differentiation. Positive for epithelial cells of cornea, snout and some oral mucosa. This antibody has been used for studying corneal epithelial stem cells
Reactivity Bovine, Human, Rabbit
Applications WB
Form Purified (Ion-exchange), in PBS containing 1% BSA and 0.1% sodium-azide
Storage 2-8C for immediate use, or at -2°C (aliquot)
References Cooper, D. et al. (1985) Lab Invest 52: 243-256Schermer, A. et al. (1986) J. Cell Biol. 103: 49-62Sun, T.-T.et al. (1984) The Cancer Cell 1: 169-176Moll R et al. (1982) Cell 31: 11-24
Background The protein encoded by this gene is a member of the keratin gene family. The type II cytokeratins consist of basic or neutral proteins which are arranged in pairs of heterotypic keratin chains coexpressed during differentiation of simple and stratified epithelial tissues. This type II cytokeratin is specifically expressed in the corneal epithelium with family member KRT12 and mutations in these genes have been associated with Meesmann's Corneal Dystrophy. The type II cytokeratins are clustered in a region of chromosome 12q12-q13.
Supplier ARP

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